EP1867625A4 - Procédé servant à produire du 3-méthyl-2-buténoate de 2-isopropényl-5-méthyl-4-hexén-1-yle - Google Patents

Procédé servant à produire du 3-méthyl-2-buténoate de 2-isopropényl-5-méthyl-4-hexén-1-yle

Info

Publication number
EP1867625A4
EP1867625A4 EP06730408A EP06730408A EP1867625A4 EP 1867625 A4 EP1867625 A4 EP 1867625A4 EP 06730408 A EP06730408 A EP 06730408A EP 06730408 A EP06730408 A EP 06730408A EP 1867625 A4 EP1867625 A4 EP 1867625A4
Authority
EP
European Patent Office
Prior art keywords
methyl
hexen
isopropenyl
butenoate
producing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP06730408A
Other languages
German (de)
English (en)
Other versions
EP1867625B1 (fr
EP1867625A1 (fr
Inventor
Katsuji Ujita
Junko Sato
Takashi Fukumoto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kuraray Co Ltd
Original Assignee
Kuraray Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kuraray Co Ltd filed Critical Kuraray Co Ltd
Publication of EP1867625A1 publication Critical patent/EP1867625A1/fr
Publication of EP1867625A4 publication Critical patent/EP1867625A4/fr
Application granted granted Critical
Publication of EP1867625B1 publication Critical patent/EP1867625B1/fr
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/63—Esters of sulfonic acids
    • C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
    • C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
    • C07C309/66—Methanesulfonates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/26—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids
    • C07C303/28—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids by reaction of hydroxy compounds with sulfonic acids or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/10—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with ester groups or with a carbon-halogen bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Il est exposé un procédé servant à produire de façon industriellement avantageuse du 3-méthyl-2-buténoate de 2-isopropényl-5-méthyl-4-hexén-1-yle avec un rendement de production élevé. Il est précisément exposé un procédé servant à produire du 3-méthyl-2-buténoate de 2-isopropényl-5-méthyl-4-hexén-1-yle représenté par la formule (IV) ci-dessous lequel est caractérisé en ce qu'on obtient un composé sulfonate représenté par la formule générale (III) ci-dessous en faisant réagir du 2-isopropényl-5-méthyl-4-hexén-1-ol avec un halogénure de sulfonyle organique en présence d'une substance basique et on fait réagir ensuite le composé sulfonate ainsi obtenu avec un acide 3-méthylcrotonique en présence d'une substance basique. (Dans la formule, R représente un groupe hydrocarboné.)
EP06730408A 2005-04-05 2006-03-29 Procédé servant à produire du 3-méthyl-2-buténoate de 2-isopropényl-5-méthyl-4-hexén-1-yle Not-in-force EP1867625B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2005108699 2005-04-05
PCT/JP2006/306460 WO2006109570A1 (fr) 2005-04-05 2006-03-29 Procédé servant à produire du 3-méthyl-2-buténoate de 2-isopropényl-5-méthyl-4-hexén-1-yle

Publications (3)

Publication Number Publication Date
EP1867625A1 EP1867625A1 (fr) 2007-12-19
EP1867625A4 true EP1867625A4 (fr) 2009-08-12
EP1867625B1 EP1867625B1 (fr) 2010-10-20

Family

ID=37086852

Family Applications (1)

Application Number Title Priority Date Filing Date
EP06730408A Not-in-force EP1867625B1 (fr) 2005-04-05 2006-03-29 Procédé servant à produire du 3-méthyl-2-buténoate de 2-isopropényl-5-méthyl-4-hexén-1-yle

Country Status (7)

Country Link
US (1) US8097746B2 (fr)
EP (1) EP1867625B1 (fr)
JP (1) JP5001144B2 (fr)
DE (1) DE602006017670D1 (fr)
ES (1) ES2351421T3 (fr)
WO (1) WO2006109570A1 (fr)
ZA (1) ZA200709013B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5009306B2 (ja) * 2006-12-19 2012-08-22 株式会社クラレ ２−イソプロペニル−５−メチル−４−ヘキセン−１−イル３−メチル−２−ブテノアートの製造方法
CN103688959B (zh) * 2014-01-04 2015-04-22 福建省农业科学院植物保护研究所 3-二辛硫基-1,1,1-三氟-2-丙烷与生物农药联合作用防治小菜蛾的方法
US9738587B2 (en) 2014-12-02 2017-08-22 Shin-Etsu Chemical Co., Ltd. Method for producing 2-isopropenyl-5-methyl-4-hexen-1-yl 3-methyl-2-butenoate

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1244188A (en) * 1968-01-10 1971-08-25 Givaudan & Cie Sa LAVANDULIC ACID NITRILE AND LAVANDULYL beta-beta-DIMETHYLACRYLATE

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3666789A (en) * 1969-05-21 1972-05-30 Sumitomo Chemical Co Cyclopropanecarboxylic acid esters
HU195178B (en) 1986-04-11 1988-04-28 Egyt Gyogyszervegyeszeti Gyar Process for producing (+)-13-norfaranal of tracer activity for monomorium pharaonis

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1244188A (en) * 1968-01-10 1971-08-25 Givaudan & Cie Sa LAVANDULIC ACID NITRILE AND LAVANDULYL beta-beta-DIMETHYLACRYLATE

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
MILLAR, JOCELYN G. ET AL: "Development and optimization of methods for using sex pheromone for monitoring the mealybug Planococcus ficus (Homoptera: Pseudococcidae) in California vineyards", JOURNAL OF ECONOMIC ENTOMOLOGY , 95(4), 706-714 CODEN: JEENAI; ISSN: 0022-0493, 2002, XP002535532 *
See also references of WO2006109570A1 *

Also Published As

Publication number Publication date
WO2006109570A1 (fr) 2006-10-19
ZA200709013B (en) 2009-01-28
DE602006017670D1 (de) 2010-12-02
US20090023941A1 (en) 2009-01-22
EP1867625B1 (fr) 2010-10-20
JPWO2006109570A1 (ja) 2008-10-30
ES2351421T3 (es) 2011-02-04
US8097746B2 (en) 2012-01-17
EP1867625A1 (fr) 2007-12-19
JP5001144B2 (ja) 2012-08-15

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Inventor name: FUKUMOTO, TAKASHI, C/O KURARAY CO., LTD.

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